Canonical Allele Identifier: PA2826278055
Gene: USB1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191840.1:p.Met116Arg
CA396129119
NM_001204911.2:c.347T>G